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In situ splitting after selective partial portal vein ligation or simultaneous hepatic artery ligation promotes liver regeneration

This study seeks to compare the impact of selective partial portal vein ligation (PPVL) or the combination of simultaneous hepatic artery ligation (PPVAL) with in situ splitting (ISS) on liver regeneration and injury. Rats were randomized into three groups; namely: selective PVL, PPVL + ISS and PPVA...

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Autores principales: Yao, Li-Bin, Li, Chong-Hui, Wu, Xiao-Juan, Wang, Xue-Dong, Ge, Xin-Lan, Zhang, Ai-Qun, Zhu, Xiao-Cheng, Shao, Yong, Dong, Jia-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992145/
https://www.ncbi.nlm.nih.gov/pubmed/29880798
http://dx.doi.org/10.1038/s41598-018-26742-5
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author Yao, Li-Bin
Li, Chong-Hui
Wu, Xiao-Juan
Wang, Xue-Dong
Ge, Xin-Lan
Zhang, Ai-Qun
Zhu, Xiao-Cheng
Shao, Yong
Dong, Jia-Hong
author_facet Yao, Li-Bin
Li, Chong-Hui
Wu, Xiao-Juan
Wang, Xue-Dong
Ge, Xin-Lan
Zhang, Ai-Qun
Zhu, Xiao-Cheng
Shao, Yong
Dong, Jia-Hong
author_sort Yao, Li-Bin
collection PubMed
description This study seeks to compare the impact of selective partial portal vein ligation (PPVL) or the combination of simultaneous hepatic artery ligation (PPVAL) with in situ splitting (ISS) on liver regeneration and injury. Rats were randomized into three groups; namely: selective PVL, PPVL + ISS and PPVAL + ISS. The changes in hepatic hemodynamics, liver regeneration and hepatocytic injury were examined. Blood flow to the left portal branch and the microcirculation of the left median lobe after PPVL or PPVAL was significantly reduced. Liver regeneration of PPVAL + ISS group was more pronounced than that in the PPVL + ISS and PVL groups at 48 and 72 hours as well as 7 d postoperatively. The serum biochemical markers and histopathological examination demonstrated reduced levels of liver injury in the PPVL + ISS group. Injury to hepatocytes was more pronounced with PPVAL + ISS than PVL. HGF, TNF-α and IL-6 expression in the regenerated lobes in both PPVAL + ISS and PPVL + ISS groups increased significantly when compared to the PVL group. We demonstrated that both PPVL + ISS and PPVAL + ISS were effective and feasible means of inducing remnant liver hypertrophy and could serve as a rapid clinical application for qualified patients.
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spelling pubmed-59921452018-06-21 In situ splitting after selective partial portal vein ligation or simultaneous hepatic artery ligation promotes liver regeneration Yao, Li-Bin Li, Chong-Hui Wu, Xiao-Juan Wang, Xue-Dong Ge, Xin-Lan Zhang, Ai-Qun Zhu, Xiao-Cheng Shao, Yong Dong, Jia-Hong Sci Rep Article This study seeks to compare the impact of selective partial portal vein ligation (PPVL) or the combination of simultaneous hepatic artery ligation (PPVAL) with in situ splitting (ISS) on liver regeneration and injury. Rats were randomized into three groups; namely: selective PVL, PPVL + ISS and PPVAL + ISS. The changes in hepatic hemodynamics, liver regeneration and hepatocytic injury were examined. Blood flow to the left portal branch and the microcirculation of the left median lobe after PPVL or PPVAL was significantly reduced. Liver regeneration of PPVAL + ISS group was more pronounced than that in the PPVL + ISS and PVL groups at 48 and 72 hours as well as 7 d postoperatively. The serum biochemical markers and histopathological examination demonstrated reduced levels of liver injury in the PPVL + ISS group. Injury to hepatocytes was more pronounced with PPVAL + ISS than PVL. HGF, TNF-α and IL-6 expression in the regenerated lobes in both PPVAL + ISS and PPVL + ISS groups increased significantly when compared to the PVL group. We demonstrated that both PPVL + ISS and PPVAL + ISS were effective and feasible means of inducing remnant liver hypertrophy and could serve as a rapid clinical application for qualified patients. Nature Publishing Group UK 2018-06-07 /pmc/articles/PMC5992145/ /pubmed/29880798 http://dx.doi.org/10.1038/s41598-018-26742-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yao, Li-Bin
Li, Chong-Hui
Wu, Xiao-Juan
Wang, Xue-Dong
Ge, Xin-Lan
Zhang, Ai-Qun
Zhu, Xiao-Cheng
Shao, Yong
Dong, Jia-Hong
In situ splitting after selective partial portal vein ligation or simultaneous hepatic artery ligation promotes liver regeneration
title In situ splitting after selective partial portal vein ligation or simultaneous hepatic artery ligation promotes liver regeneration
title_full In situ splitting after selective partial portal vein ligation or simultaneous hepatic artery ligation promotes liver regeneration
title_fullStr In situ splitting after selective partial portal vein ligation or simultaneous hepatic artery ligation promotes liver regeneration
title_full_unstemmed In situ splitting after selective partial portal vein ligation or simultaneous hepatic artery ligation promotes liver regeneration
title_short In situ splitting after selective partial portal vein ligation or simultaneous hepatic artery ligation promotes liver regeneration
title_sort in situ splitting after selective partial portal vein ligation or simultaneous hepatic artery ligation promotes liver regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992145/
https://www.ncbi.nlm.nih.gov/pubmed/29880798
http://dx.doi.org/10.1038/s41598-018-26742-5
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